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A novel mutation in the RS1 gene in a Chinese family with X-linked congenital retinoschisis
The purpose of the present study was to assess the clinical characteristics of X-linked retinoschisis (XLRS) in a Chinese family over a 7-year period with the aim of identifying possible genetic mutations associated with this disease. A total of 2 male siblings from a family with XLRS were followed...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
D.A. Spandidos
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7739845/ https://www.ncbi.nlm.nih.gov/pubmed/33335587 http://dx.doi.org/10.3892/etm.2020.9556 |